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Marijuana in Combination With Opioids in Palliative and Hospice Patients

Primary Purpose

Pain

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Medical Marijuana
Sponsored by
The Connecticut Hospice Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Pain focused on measuring pain management, terminally ill

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age > 18
  • Alert adults
  • requiring opioids for pain management (routine or as needed)
  • cancer diagnosis or non-cancer diagnosis as their terminal illness

Exclusion Criteria:

  • pregnant women
  • Age < 18
  • minimally or unresponsive patients unable to take oral medications
  • agitated combative patients

Sites / Locations

  • The Connecticut Hospice Inc.

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Single treatment arm

Arm Description

marijuana adjuvant treatment group utilizing scheduled opioid therapy in inpatient hospice hospital setting

Outcomes

Primary Outcome Measures

primary reduction of pain and reduction in overall opioid utilization
numeric pain scale

Secondary Outcome Measures

improvement in overall patient well being
modified Edmonton Assessment Scale
weight stabilization with increased appetite
modified Edmonton Assessment Scale
improved oxygen saturation
modified Edmonton Assessment Scale
improvement or prevention of nausea and vomiting
modified Edmonton Assessment Scale

Full Information

First Posted
July 26, 2017
Last Updated
September 1, 2022
Sponsor
The Connecticut Hospice Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT03233633
Brief Title
Marijuana in Combination With Opioids in Palliative and Hospice Patients
Official Title
Marijuana in Combination With Opioids for Pain and Symptom Control in Hospice Patients
Study Type
Interventional

2. Study Status

Record Verification Date
September 2022
Overall Recruitment Status
Completed
Study Start Date
May 10, 2017 (Actual)
Primary Completion Date
August 5, 2022 (Actual)
Study Completion Date
August 5, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The Connecticut Hospice Inc.

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Study Objectives: Primary reduction of pain and reduction in overall opioid utilization. Secondary improvement in overall patient well being, weight stabilization with increased appetite, improved oxygen saturation, improvement or prevention of nausea and vomiting. Study Rationale: To determine optimum use and dosing of medical marijuana (CBD:THC) for pain and symptom management. Study Population: This study specifically will enroll cancer and non-cancer patients as a primary diagnosis suffering from pain and having a terminal illness (defined as having less than 6 months to live) requiring end of life care.
Detailed Description
Primary Endpoint: Death or discharge Secondary and Exploratory endpoints:Secondary improvement in overall patient well being, weight stabilization with increased appetite, improved oxygen saturation, improvement or prevention of nausea and vomiting. Study design: This will be an open-label study. Patients will choose to participate in a Marijuana adjuvant treatment group, receiving marijuana in combination with standard opioid therapy. Subject number: Minimum 66 patients Treatment Duration: Minimum 5 days Duration of follow up: Patients' initial opioid dose, dosing schedule and numeric pain score will be recorded. For the duration of the study (at least five days) changes in opioid doses and numeric pain scores will be tracked daily. Marijuana will be administered to the patient via oral route three times daily for at least five days. Patients will receive standardized CBD:THC product provided by NIDA. On admission to the study, a modified Edmonton Symptom assessment scale to quantify baseline appetite, depression, nausea, vomiting, overall well-being, and anxiety. Data Tracking: Primary objective tracking will include average numeric pain scores and number of opioid dosage increases and average daily opioid amount (mg equivalents of morphine). Secondary objectives include Weight, Appetite, N/V, O2 Saturation, Self-reported data points from the modified Edmonton Assessment Scale.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pain
Keywords
pain management, terminally ill

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
66 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Single treatment arm
Arm Type
Other
Arm Description
marijuana adjuvant treatment group utilizing scheduled opioid therapy in inpatient hospice hospital setting
Intervention Type
Drug
Intervention Name(s)
Medical Marijuana
Other Intervention Name(s)
cannabidiol, medical cannabis
Intervention Description
oral capsule, high ratio CBD:THC
Primary Outcome Measure Information:
Title
primary reduction of pain and reduction in overall opioid utilization
Description
numeric pain scale
Time Frame
minumum 5 days
Secondary Outcome Measure Information:
Title
improvement in overall patient well being
Description
modified Edmonton Assessment Scale
Time Frame
minimum 5 days
Title
weight stabilization with increased appetite
Description
modified Edmonton Assessment Scale
Time Frame
minimum 5 days
Title
improved oxygen saturation
Description
modified Edmonton Assessment Scale
Time Frame
minimum 5 days
Title
improvement or prevention of nausea and vomiting
Description
modified Edmonton Assessment Scale
Time Frame
minimum 5 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age > 18 Alert adults requiring opioids for pain management (routine or as needed) cancer diagnosis or non-cancer diagnosis as their terminal illness Exclusion Criteria: pregnant women Age < 18 minimally or unresponsive patients unable to take oral medications agitated combative patients
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Theodore Zanker, MD
Organizational Affiliation
The Connecticut Hospice Inc.
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Connecticut Hospice Inc.
City
Branford
State/Province
Connecticut
ZIP/Postal Code
06405
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Marijuana in Combination With Opioids in Palliative and Hospice Patients

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